FDA Inspection 1081761 - Kulzer SRL - February 13, 2019

FDA Inspection 1081761 for Kulzer SRL on February 13, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1081761 for Kulzer SRL on February 13, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

Kulzer SRL

Inspection Date

February 13, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa0da22e-8005-4225-9208-66ffedda936c

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